EP0067257A1 - Heat radiation reflecting glass and preparation thereof - Google Patents

Heat radiation reflecting glass and preparation thereof Download PDF

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Publication number
EP0067257A1
EP0067257A1 EP81302669A EP81302669A EP0067257A1 EP 0067257 A1 EP0067257 A1 EP 0067257A1 EP 81302669 A EP81302669 A EP 81302669A EP 81302669 A EP81302669 A EP 81302669A EP 0067257 A1 EP0067257 A1 EP 0067257A1
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Prior art keywords
nickel
salt
copper
alloy layer
solution
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EP81302669A
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German (de)
French (fr)
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EP0067257B1 (en
Inventor
Takayuki Kobayashi
Ryo Tamamura
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AGC Inc
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Asahi Glass Co Ltd
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Priority to DE8181302669T priority Critical patent/DE3173705D1/en
Priority to EP81302669A priority patent/EP0067257B1/en
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    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C18/00Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
    • C23C18/16Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by reduction or substitution, e.g. electroless plating
    • C23C18/48Coating with alloys
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C17/00Surface treatment of glass, not in the form of fibres or filaments, by coating
    • C03C17/06Surface treatment of glass, not in the form of fibres or filaments, by coating with metals
    • C03C17/10Surface treatment of glass, not in the form of fibres or filaments, by coating with metals by deposition from the liquid phase

Definitions

  • the present invention relates to a heat radiating reflecting glass having excellent characteristics of high heat radiation reflectivity and excellent durability.
  • the heat radiation reflecting glasses having a metal layer formed by a chemical plating have an advantage of a low cost, because an economical apparatus can be used for the preparation in comparison with a vacuum deposition process or a sputtering process.
  • a product having a copper layer has the optimum heat radiation reflectivity, however, it has not satisfactory corrosion resistance to have not a desired durability.
  • a product having a nickel layer has a desired corrosion resistance and enough durability but has inferior heat radiation reflectivity to that of the copper layer.
  • a heat radiation reflecting glass having a transparent nickel-copper alloy layer formed by depositing said nickel-copper alloy on a glass plate by a chemical plating process whereby imparting advantages of both of a nickel component and a copper component to give excellent heat radiation reflectivity of K value (heat-transfer coefficient) of upto 2.0 and SC (shading coefficient) of upto 0.20 and excellent corrosion resistance in a low cost.
  • the transparent nickel-copper alloy layer formed by the chemical plating process preferably comprises 1 to 25 wt. % of Ni component and 75 to 99 wt. % of Cu component.
  • Ni content is more than 25 wt. %, the heat radiation reflectivity is disadvantageously too low whereas when it is less than 1 wt. %, the corrosion resistance is not satisfactory.
  • Cu content is more than 99 wt. %, the corrosion resistance is not satisfactory whereas when it. is less than 75 Wt.%, the heat radiation reflectivity is disadvantageously too low.
  • the Pd content is preferably upto 100 ppm especially 2 to 80 ppm by weight based on the alloy layer.
  • the ratio of the Ni component is disadvantageously excess whereas it is less than 1 ppm, the ratio of the Ni component is disadvantageously remarkably low.
  • the ratio of Ni component can be controlled to 1 to 25 wt. %.
  • the transparent nickel-copper-boron alloy layer preferably comprises 1 to 20 wt. % Ni component, 75 to 99 wt.% of Cu component and upto 5 wt. % of B component; especially 1 to 10 wt. % of Ni component, 89 to 99 wt.% of Cu component and 0.001 to 1 wt. % of B component.
  • the heat radiation reflectivity is disadvantageously low.
  • the advantages of both of the Ni component and the Cu component have been imparted by the combination of the Ni component, the Cu component and the B component to give the heat radiation reflecting glass having excellent heat radiation reflectivity such as a heat-transfer coefficient (K value) of upto 2.0 and a shading coefficient (SC) of upto 0.20 and excellent corrosion resistance.
  • K value heat-transfer coefficient
  • SC shading coefficient
  • the transparent nickel-copper alloy layer of the present invention preferably has a thickness of 50 to 1000 ⁇ especially 100 to 700 A so as to impart a desired transparency and desired optical characteristics such as heat radiation reflectivity and transmissivity.
  • a hue of the nickel-copper alloy layer of the present invention can be controlled in a range of neutral to copper color by selecting the Ni content.
  • the neutral color is given by increasing the Ni content whereas the copper color is given by decreasing the Ni content.
  • the nickel-copper alloy layer of the present invention means a layer comprising a nickel-copper alloy as the main component and includes the nickel-copper alloy layer containing Pd component and the Ni-Cu-B alloy layer or the alloy layer containing a small amount of the other component.
  • a nickel salt, a copper salt and a reducing agent for reducing said nickel salt and said copper salt are applied in the presence of the Pd salt on the surface of the glass plate to chemically reduce said nickel salt and said copper salt to form the nickel-copper alloy layer.
  • the nickel-copper alloy layer is formed by the following steps.
  • the step (4) of the preparation of the nickel-copper alloy layer is substituted by the following step.
  • the nickel salt, the copper salt and an alkali borohydride or a borane amine as a reducing agent for the nickel salt and the copper. salt are applied in the presence of the palladium salt to chemically deposit the nickel-copper-boron alloy layer.
  • the following processes can be considered as the process for applying the nickel salt, the copper salt and the reducing agent in the presence of the palladium salt on the glass plate.
  • the solution of the nickel salt and the solution of the copper salt used for the formation of the nickel-copper alloy layer various formulations for the nickel salt and the copper salt can be used.
  • the solution of the nickel salt it is possible to use a solution of an inorganic or organic nickel salt such as nickel chloride, nickel sulfate, nickel acetate or a mixture of two or more nickel salts and a chelating agent such as Rochelle salt, EDTA,EDTA-2Na, sodium citrate and sodium gluconate; a pH buffering agent and a pH modifier or the solution containing a desired additive especially,an aqueous solution.
  • an inorganic or organic nickel salt such as nickel chloride, nickel sulfate, nickel acetate or a mixture of two or more nickel salts and a chelating agent such as Rochelle salt, EDTA,EDTA-2Na, sodium citrate and sodium gluconate
  • a pH buffering agent and a pH modifier or the solution containing a desired additive especially,an aqueous solution.
  • the solution of the copper salt it is possible to use a solution of a copper salt such as copper nitrate, copper sulfate, copper acetate or a mixture of two or more copper salts and a chelating agent, a pH buffering agent and a pH modifier if necessary, a desired additive as used in the nickel solution, especially an aqueous solution.
  • a copper salt such as copper nitrate, copper sulfate, copper acetate or a mixture of two or more copper salts and a chelating agent, a pH buffering agent and a pH modifier if necessary, a desired additive as used in the nickel solution, especially an aqueous solution.
  • the solution of the palladium salt it is possible to use a solution of a palladium salt such as palladium chloride, palladium nitrate and palladium sulfate, especially an aqueous solution of the palladium salt.
  • a palladium salt such as palladium chloride, palladium nitrate and palladium sulfate, especially an aqueous solution of the palladium salt.
  • a concentration of the nickel salt in the nickel salt solution is preferably in a range of 0.01 to 1% and a concentration of the copper salt in the copper salt solution is preferably in a range of 0,02 to 2%,
  • the reducing agent solution is a solution of a reducing agent for reducing the nickel salt and the copper salt to form the nickel-copper alloy layer such as solutions of formaldehyde, reducing sugars, Rochelle salt, tartaric acid or sodium hypophosphite especially the aqueous solution.
  • the spraying process is the optimum as the process for applying these solutions on the glass plate. It is especially preferable to apply these solutions at the same time.
  • the palladium salt is present in the deposition of the metals by reducing the copper salt and the nickel salt whereby the nickel-copper alloy layer can be effectively formed by the effect of the palladium salt.
  • the palladium salt is not present, it is not easy to deposit nickel component and it is not easy to form a nickel-copper alloy layer containing 1 to 25 wt.% of nickel component,
  • the palladium salt at a concentration of 1 to 100 ppm in the solution for plating nickel and copper.
  • the ratio of Ni component in the alloy layer is too much and the heat reflectivity is disadvantageously low ' whereas when it is less than 1 ppm, the ratio of Ni component in the alloy layer is too small, and the durability of the alloy layer is disadvantageously inferior,
  • the boron compound is used as the reducing agent to apply it in the formation of the alloy layer,
  • the boron compound is preferably to reduce the nickel salt and the copper salt sometimes the palladium salt to form the nickel-copper-boron alloy layer so as to incorporate the boron component in the nickel-copper layer. It is optimum to use alkali borohydride and borane amine.
  • the alkali borohydrides can be sodium borohydride, potassium borohydride and lithium borohydride.
  • the borane amines can be borane amine, borane dimethylamine, borane diethylamine and borane trimethylamine.
  • a time for chemical plating in the deposition of the nickel-copper alloy layer is preferably.in a range of 30 second to 20 minute especially about 1 minute to 10 minute.
  • a temperature of the solutions of the nickel salt, the copper salt and the palladium salt, the solution of the reducing agent or the solution of these salts and the reducing agent is preferably in a range of 10 to 60°C especially about 30°C .
  • Velocities for depositions of the nicekl salt and the copper salt are different depending upon the variation of the temperature in the chemical plating. It'is important to maintain the temperature in the chemical plating to be ⁇ 3°C in view of the prevention of color ununiformity.
  • a temperature of the substrate in the chemical plating is preferably in a range of 10 to 60°C especially about room temperature.
  • a spraying rate and a plating time are selected so as to obtain a desired thickness of the alloy layer.
  • a protective coating or the other functional layer as a top coating on the nickel-copper alloy layer formed on the glass plate or to carry out a chemical treatment, or to form an adhesive coating or the other functional layer as an under coating.
  • the glass plate can be made of normal glass or heat radiation absorbing glass or other various glasses and also organic glasses such as polycarbonate and methacrylate.
  • a glass plate (300 mm x 300 mm x 5 mm) was polished with ceria and rinsed with water.
  • An aqueous solution of stannous chloride (SnCl 2 : 0.8 g/1 liter of water) was sprayed on the surface of the glass plate at a rate of 5 liter/m2 to perform a sensitizing treatment and then, the glass plate was rinsed with water and an aqueous solution of palladium chloride (PdCl 2 :0.05 g/1 liter of water) was sprayed on the surface of the glass plate at a rate of 5 liter/m 2 to perform an activating treatment.
  • SnCl 2 0.8 g/1 liter of water
  • the following solution A and the solution B 1 were respectively sprayed on the treated surface of the glass plate by each spray-gun at a volumetric ratio of 1 : 1 at each rate of 5 liter/m 2 and they were kept for 6 minutes to deposit a nickel-copper alloy layer on the glass plate by a chemical plating process.
  • the resulting nickel-copper alloy layer had a thickness of 500 ⁇ and a ratio of Ni to Cu of 1 : 99 by weight. In the nickel-copper alloy layer, any Pd component was not found.
  • a glass plate (300 mm x 300 mm x 5 mm) was polished with c eria and rinsed with water.
  • An aqueous solution of stannous chloride . (SnCl 2 : 0.8 g/l liter of water) was sprayed on the surface of the glass plate at a rate of 5 liter/m 2 to perform a sensitizing treatment and then, the glass plate was rinsed with water and an aqueous solution of palladium chloride (PdCl 2 : 0.05 g/l liter of water) was sprayed on the surface of the glass plate at a rate of 5 liter/m 2 to perform an activating treatment.
  • PdCl 2 palladium chloride
  • the resulting nickel-copper-palladium alloy layer had a thickness of 500 A and a ratio of Ni to Cu of 7 : 93 by weight and a content of Pd component of 10 ppm.
  • the characteristics of the layer were measured. The results are shown in Table 1. The optical characteristic is shown in Figure 1 c.
  • a glass plate (300 mm x 300 mm x 5 mm) was polished with ceria and rinsed with water.
  • An aqueous solution of stannous chloride (SnCl 2 : 0.8 g/1 liter of water) was sprayed on the surface of the glass plate at a rate of 5 liter/m 2 to perform a sensitizing treatment and then, the glass plate was rinsed with water and an aqueous solution of palladium chloride (PdCl 2 :0.05 g/1 liter of water) was sprayed on the surface of the glass plate at a rate of 5 liter/m 2 to perform an activating treatment.
  • SnCl 2 0.8 g/1 liter of water
  • the following solution A3 and the solution B 3 were respectively sprayed on the treated surface of the glass plate by each spray-gun at a volumetric ratio of 1 : 1 at each rate of 5 liter/m 2 and they were kept for 6 minutes to deposit a nickel-copper-boron alloy layer on the glass plate by a chemical plating process.
  • the resulting nickel-copper-boron alloy layer had a thickness of 500 A and comprised 3.4 wt.% of Ni, 96.5 wt.% of Cu and 0.1 wt.% of B.
  • the characteristics of the layer were measured. The results are shown in Table 1. The optical characteristic is shown in Figure 1 c'.
  • the resulting nickel-copper-boron alloy layer had a thickness of 500 ⁇ and comprised 2.0 wt.% of Ni and 97.9 wt.% of Cu and 0.1 wt.% of B,
  • the durability test result of the layer is shown in Table 1.
  • Example 3 In accordance with the process of Example 3 except using Solution A 5 and Solution B 5 , a nickel-copper-boron alloy layer was formed.
  • the resulting nickel-copper-boron alloy layer had a 0 thickness of 500 A and comprised 3.2 wt.% of Ni, 96.6 wt.% of Cu and 0.2 wt.% of B.
  • the durability test result of the layer is shown in Table 1.
  • a glass plate (300 mm x 300 mm x 5 mm) was polished with ceria and rinsed with water.
  • An aqueous solution of stannous chloride (SnCl 2 : 0.8 g/1 liter of water) was sprayed on the surface of the glass plate at a rate of 5 liter/m 2 to perform a sensitizing treatment and then, the glass plate was rinsed with water and an aqueous solution of palladium chloride (PdCl 2 :0.05 g/l liter of water) was sprayed on the surface of the glass plate at a rate of 5 liter/m 2 to perform an activating treatment.
  • SnCl 2 0.8 g/1 liter of water
  • solution A 6 and the solution B 6 were respectively sprayed on the treated surface of the glass plate by each spray-gun at a volumetric ratio of 1 : 1 at each rate of 5 liter/m2 and they were kept for 6 minutes to deposit a metal layer on the glass plate by a chemical plating process.
  • the resulting metal layer had a thickness of 500 A and comprised about 100% of Cu (Ni was not substantially included). The characteristics of the layer were measured. The results are. shown in Table 1.
  • Solution A 7 and Solution B 7 were respectively sprayed by each spray-gun at a volumetric ratio of about 1 : 1 at each rate of 5 liter/m 2 and they were kept for 2 minutes to deposit a nickel-boron alloy layer on the glass plate by a chemical plating.
  • the resulting nickel-boron alloy layer had a thickness of 0 500 A .
  • the characteristics of the nickel-boron layer were measured. The results are shown in Table 1.
  • the resulting copper-boron alloy layer had a thickness of 500 ⁇ .
  • the heat radiation reflecting glass of the present invention had superior thermal characteristics such as heat passing coefficient and shading coefficient to those of the conventional heat-transfer reflecting glass having a nickel-boron alloy layer and also had superior durability to those of the copper layer and had neutral hue to be desirable as a heat, radiation reflecting glass.
  • the durability was determined by an observation of degree of corrosion after maintaining at 30°C RH of 70% for one month, ⁇ : non-corrosion X : corrosion
  • the visible transmissivity (Tv) was measured under the light incidence from each layer of the sample of glass plate having a thickness of 5 mm.
  • the visible reflectivity (Rv) was measured under the light incidence from the non-coated side of a glass plate coated with the layer having a thickness of 5 mm.
  • the heat-transfer coefficient (K value) and the shading coefficient (SC) were measured for an insulating glass unit prepared by a pair of glass plates having a thickness of 5 mm and an air space of 12 mm.

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Abstract

A heat radiation reflecting glass comprises a transparent nickel-copper alloy layer formed by a chemical plating process on a glass plate.

Description

    BACKGROUND OF THE INVENTION: FIELD OF THE INVENTION:
  • The present invention relates to a heat radiating reflecting glass having excellent characteristics of high heat radiation reflectivity and excellent durability.
  • DESCRIPTION OF THE PRIOR ARTS:
  • Glass plates having each thin transparent or translucent metal layer made of silver, nickel or aluminum which reflect or intercept heat radiation of solar or radiant heat have been known as heat radiation reflecting glass plates and have been used as a single glass plate, an insulating glass unit or a laminated glass plate in buildings, vehicles and various apparatuses and instruments. The heat radiation reflecting glasses having a metal layer formed by a chemical plating have an advantage of a low cost, because an economical apparatus can be used for the preparation in comparison with a vacuum deposition process or a sputtering process. Among the chemical coating process, a product having a copper layer has the optimum heat radiation reflectivity, however, it has not satisfactory corrosion resistance to have not a desired durability. On the other hand, a product having a nickel layer has a desired corrosion resistance and enough durability but has inferior heat radiation reflectivity to that of the copper layer.
  • SUMMARY OF THE INVENTION:
  • It is an object of the present invention to provide a heat radiation reflecting glass prepared by a chemical plating process which has not the above-mentioned disadvantages.
  • The foregoing and other objects of the present invention have been attained by providing a heat radiation reflecting glass having a transparent nickel-copper alloy layer formed by depositing said nickel-copper alloy on a glass plate by a chemical plating process whereby imparting advantages of both of a nickel component and a copper component to give excellent heat radiation reflectivity of K value (heat-transfer coefficient) of upto 2.0 and SC (shading coefficient) of upto 0.20 and excellent corrosion resistance in a low cost.
  • DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS:
  • The transparent nickel-copper alloy layer formed by the chemical plating process preferably comprises 1 to 25 wt. % of Ni component and 75 to 99 wt. % of Cu component.
  • When Ni content is more than 25 wt. %, the heat radiation reflectivity is disadvantageously too low whereas when it is less than 1 wt. %, the corrosion resistance is not satisfactory. When Cu content is more than 99 wt. %, the corrosion resistance is not satisfactory whereas when it. is less than 75 Wt.%, the heat radiation reflectivity is disadvantageously too low.
  • It is preferable to incorporate Pd component in the transparent nickel-copper alloy layer. The Pd content is preferably upto 100 ppm especially 2 to 80 ppm by weight based on the alloy layer. When the Pd content is more than 100 ppm, the ratio of the Ni component is disadvantageously excess whereas it is less than 1 ppm, the ratio of the Ni component is disadvantageously remarkably low. Thus, the ratio of Ni component can be controlled to 1 to 25 wt. %.
  • It is possible to incorporate a boron component in the transparent nickel-copper alloy layer. The transparent nickel-copper-boron alloy layer preferably comprises 1 to 20 wt. % Ni component, 75 to 99 wt.% of Cu component and upto 5 wt. % of B component; especially 1 to 10 wt. % of Ni component, 89 to 99 wt.% of Cu component and 0.001 to 1 wt. % of B component.
  • When the B content is more than 5 wt.%, the heat radiation reflectivity is disadvantageously low. The advantages of both of the Ni component and the Cu component have been imparted by the combination of the Ni component, the Cu component and the B component to give the heat radiation reflecting glass having excellent heat radiation reflectivity such as a heat-transfer coefficient (K value) of upto 2.0 and a shading coefficient (SC) of upto 0.20 and excellent corrosion resistance. Of course, it is preferable to incorporate upto 100 ppm of the Pd component in the transparent Ni-Cu-B alloy layer from the above-mentioned viewpoint.
  • The transparent nickel-copper alloy layer of the present invention preferably has a thickness of 50 to 1000 å especially 100 to 700 A so as to impart a desired transparency and desired optical characteristics such as heat radiation reflectivity and transmissivity.
  • A hue of the nickel-copper alloy layer of the present invention can be controlled in a range of neutral to copper color by selecting the Ni content. For example, the neutral color is given by increasing the Ni content whereas the copper color is given by decreasing the Ni content.
  • The nickel-copper alloy layer of the present invention means a layer comprising a nickel-copper alloy as the main component and includes the nickel-copper alloy layer containing Pd component and the Ni-Cu-B alloy layer or the alloy layer containing a small amount of the other component.
  • In the preparation of the transparent nickel-copper alloy layer on the glass plate, a nickel salt, a copper salt and a reducing agent for reducing said nickel salt and said copper salt are applied in the presence of the Pd salt on the surface of the glass plate to chemically reduce said nickel salt and said copper salt to form the nickel-copper alloy layer.
  • As one embodiment, the nickel-copper alloy layer is formed by the following steps.
    • (1) The surface of the glass plate is cleaned.by rinsing with water or a detergent or polishing with an abrasive such as cerium oxide.
    • (2) The surface of. the glass plate is rinsed with water preferably distilled water or deionized water after contacting it with a dilute aqueous solution of a tin salt such as stannous chloride for a short time at about room temperature.
    • (3) If necessary, the surface is further treated with a dilute aqueous solution of a palladium salt such as palladium chloride and then is rinsed with water.
    • (4) The nickel salt, the copper salt, and the reducing agent for reducing the nickel salt and the copper salt are applied in the presence of the palladium salt on the glass plate to chemically reduce the nickel salt and the copper salt at substantially the same time to deposit the nickel-copper alloy layer.
    • (5) The glass plate having the nickel-copper alloy layer is rinsed with water.
  • In the process for forming the transparent nickel-copper-boron alloy layer on the glass plate, the step (4) of the preparation of the nickel-copper alloy layer is substituted by the following step.
  • The nickel salt, the copper salt and an alkali borohydride or a borane amine as a reducing agent for the nickel salt and the copper. salt are applied in the presence of the palladium salt to chemically deposit the nickel-copper-boron alloy layer.
  • The following processes can be considered as the process for applying the nickel salt, the copper salt and the reducing agent in the presence of the palladium salt on the glass plate.
  • A process for spraying at the same time both of a solution of the nickel salt, a solution of the copper salt and a solution of. the palladium salt or both of a solution of the nickel salt and the copper salt and a solution of the reducing agent.
  • A process for spraying a mixture of three or four kinds of the solutions.
  • A process for coating a mixture of four kinds of the solutions on the glass plate by a roll coating etc.
  • A process for spraying the solution of the nickel salt, the solution of the copper salt, the solution of the palladium salt or the mixture thereof by mixing them in a spray gun in a form of a single solution. The other similar processes.
  • As the solution of the nickel salt and the solution of the copper salt used for the formation of the nickel-copper alloy layer, various formulations for the nickel salt and the copper salt can be used.
  • As the solution of the nickel salt, it is possible to use a solution of an inorganic or organic nickel salt such as nickel chloride, nickel sulfate, nickel acetate or a mixture of two or more nickel salts and a chelating agent such as Rochelle salt, EDTA,EDTA-2Na, sodium citrate and sodium gluconate; a pH buffering agent and a pH modifier or the solution containing a desired additive especially,an aqueous solution.
  • As the solution of the copper salt, it is possible to use a solution of a copper salt such as copper nitrate, copper sulfate, copper acetate or a mixture of two or more copper salts and a chelating agent, a pH buffering agent and a pH modifier if necessary, a desired additive as used in the nickel solution, especially an aqueous solution.
  • As the solution of the palladium salt, it is possible to use a solution of a palladium salt such as palladium chloride, palladium nitrate and palladium sulfate, especially an aqueous solution of the palladium salt.
  • A concentration of the nickel salt in the nickel salt solution is preferably in a range of 0.01 to 1% and a concentration of the copper salt in the copper salt solution is preferably in a range of 0,02 to 2%,
  • The reducing agent solution is a solution of a reducing agent for reducing the nickel salt and the copper salt to form the nickel-copper alloy layer such as solutions of formaldehyde, reducing sugars, Rochelle salt, tartaric acid or sodium hypophosphite especially the aqueous solution.
  • The spraying process is the optimum as the process for applying these solutions on the glass plate. It is especially preferable to apply these solutions at the same time.
  • In the process of the present invention, the palladium salt is present in the deposition of the metals by reducing the copper salt and the nickel salt whereby the nickel-copper alloy layer can be effectively formed by the effect of the palladium salt. When the palladium salt is not present, it is not easy to deposit nickel component and it is not easy to form a nickel-copper alloy layer containing 1 to 25 wt.% of nickel component,
  • It is preferable to contain the palladium salt at a concentration of 1 to 100 ppm in the solution for plating nickel and copper. When it is more than 100 ppm, the ratio of Ni component in the alloy layer is too much and the heat reflectivity is disadvantageously low ' whereas when it is less than 1 ppm, the ratio of Ni component in the alloy layer is too small, and the durability of the alloy layer is disadvantageously inferior,
  • When the transparent nickel-copper alloy layer containing boron component is formed on the glass plate, for example, the boron compound is used as the reducing agent to apply it in the formation of the alloy layer,
  • The boron compound is preferably to reduce the nickel salt and the copper salt sometimes the palladium salt to form the nickel-copper-boron alloy layer so as to incorporate the boron component in the nickel-copper layer. It is optimum to use alkali borohydride and borane amine. The alkali borohydrides can be sodium borohydride, potassium borohydride and lithium borohydride. The borane amines can be borane amine, borane dimethylamine, borane diethylamine and borane trimethylamine. When the alkali borohydride is used, any toxic gas is not generated to obtain the nickel-copper-boron alloy layer without a public pollution though a toxic gas is generated in the conventional chemical plating process using formaline etc.
  • A time for chemical plating in the deposition of the nickel-copper alloy layer is preferably.in a range of 30 second to 20 minute especially about 1 minute to 10 minute. A temperature of the solutions of the nickel salt, the copper salt and the palladium salt, the solution of the reducing agent or the solution of these salts and the reducing agent is preferably in a range of 10 to 60°C especially about 30°C . Velocities for depositions of the nicekl salt and the copper salt are different depending upon the variation of the temperature in the chemical plating. It'is important to maintain the temperature in the chemical plating to be ±3°C in view of the prevention of color ununiformity. A temperature of the substrate in the chemical plating is preferably in a range of 10 to 60°C especially about room temperature. A spraying rate and a plating time are selected so as to obtain a desired thickness of the alloy layer.
  • In the present invention, it is possible to form a protective coating or the other functional layer as a top coating on the nickel-copper alloy layer formed on the glass plate or to carry out a chemical treatment, or to form an adhesive coating or the other functional layer as an under coating.
  • The glass plate can be made of normal glass or heat radiation absorbing glass or other various glasses and also organic glasses such as polycarbonate and methacrylate.
  • The present invention will be further illustrated by certain examples and references which are provided for purposes of illustration only and are not intended to be limiting the present invention.
  • EXAMPLE 1:
  • A glass plate (300 mm x 300 mm x 5 mm) was polished with ceria and rinsed with water. An aqueous solution of stannous chloride (SnCℓ2 : 0.8 g/1 liter of water) was sprayed on the surface of the glass plate at a rate of 5 liter/m2 to perform a sensitizing treatment and then, the glass plate was rinsed with water and an aqueous solution of palladium chloride (PdCℓ2:0.05 g/1 liter of water) was sprayed on the surface of the glass plate at a rate of 5 liter/m2 to perform an activating treatment.
  • The following solution A and the solution B1 were respectively sprayed on the treated surface of the glass plate by each spray-gun at a volumetric ratio of 1 : 1 at each rate of 5 liter/m2 and they were kept for 6 minutes to deposit a nickel-copper alloy layer on the glass plate by a chemical plating process.
  • Solution A1:
  • Figure imgb0001
  • Solution B 1:
  • Figure imgb0002
  • The resulting nickel-copper alloy layer had a thickness of 500 Å and a ratio of Ni to Cu of 1 : 99 by weight. In the nickel-copper alloy layer, any Pd component was not found.
  • The characteristics of the layer were measured. The results are shown in Table 1.
  • EXAMPLE 2:
  • A glass plate (300 mm x 300 mm x 5 mm) was polished with ceria and rinsed with water. An aqueous solution of stannous chloride . (SnCℓ2: 0.8 g/l liter of water) was sprayed on the surface of the glass plate at a rate of 5 liter/m2 to perform a sensitizing treatment and then, the glass plate was rinsed with water and an aqueous solution of palladium chloride (PdCℓ2: 0.05 g/l liter of water) was sprayed on the surface of the glass plate at a rate of 5 liter/m2 to perform an activating treatment.
  • The following solution A2 and the solution of B2 were respectively sprayed on the treated surface of the glass plate by each spray-gun at a volumetric ratio of 1 : 1 at each rate of 5 liter/m2 and they were kept for 6 minutes to deposit a nickel-copper alloy layer on the glass plate by a chemical plating.
  • Solution A2:
  • Figure imgb0003
  • Solution B2:
  • Figure imgb0004
  • The resulting nickel-copper-palladium alloy layer had a thickness of 500 A and a ratio of Ni to Cu of 7 : 93 by weight and a content of Pd component of 10 ppm.
  • The characteristics of the layer were measured. The results are shown in Table 1. The optical characteristic is shown in Figure 1 c.
  • EXAMPLE 3:
  • A glass plate (300 mm x 300 mm x 5 mm) was polished with ceria and rinsed with water. An aqueous solution of stannous chloride (SnCℓ2 : 0.8 g/1 liter of water) was sprayed on the surface of the glass plate at a rate of 5 liter/m2 to perform a sensitizing treatment and then, the glass plate was rinsed with water and an aqueous solution of palladium chloride (PdCℓ2 :0.05 g/1 liter of water) was sprayed on the surface of the glass plate at a rate of 5 liter/m2 to perform an activating treatment.
  • The following solution A3 and the solution B3 were respectively sprayed on the treated surface of the glass plate by each spray-gun at a volumetric ratio of 1 : 1 at each rate of 5 liter/m2 and they were kept for 6 minutes to deposit a nickel-copper-boron alloy layer on the glass plate by a chemical plating process.
  • Solution A3:
  • Figure imgb0005
  • Solution B3:
  • Figure imgb0006
  • The resulting nickel-copper-boron alloy layer had a thickness of 500 A and comprised 3.4 wt.% of Ni, 96.5 wt.% of Cu and 0.1 wt.% of B.
  • The characteristics of the layer were measured. The results are shown in Table 1. The optical characteristic is shown in Figure 1 c'.
  • EXAMPLE 4:
  • In accordance with the process of Example 3 except usin Solution A4 and Solution B4 a nickel-copper-boron alloy layer was formed.
  • Solution A4:
  • Figure imgb0007
  • Solution B4:
  • Figure imgb0008
  • The resulting nickel-copper-boron alloy layer had a thickness of 500 Å and comprised 2.0 wt.% of Ni and 97.9 wt.% of Cu and 0.1 wt.% of B, The durability test result of the layer is shown in Table 1.
  • EXAMPLE 5:
  • In accordance with the process of Example 3 except using Solution A5 and Solution B5, a nickel-copper-boron alloy layer was formed.
  • Solution A5:
  • Figure imgb0009
  • Solution B5:
  • Figure imgb0010
  • The resulting nickel-copper-boron alloy layer had a 0 thickness of 500 A and comprised 3.2 wt.% of Ni, 96.6 wt.% of Cu and 0.2 wt.% of B. The durability test result of the layer is shown in Table 1.
  • REFERENCE 1:
  • A glass plate (300 mm x 300 mm x 5 mm) was polished with ceria and rinsed with water. An aqueous solution of stannous chloride (SnCℓ2 : 0.8 g/1 liter of water) was sprayed on the surface of the glass plate at a rate of 5 liter/m2 to perform a sensitizing treatment and then, the glass plate was rinsed with water and an aqueous solution of palladium chloride (PdCℓ2 :0.05 g/l liter of water) was sprayed on the surface of the glass plate at a rate of 5 liter/m2 to perform an activating treatment.
  • The following solution A6 and the solution B6 were respectively sprayed on the treated surface of the glass plate by each spray-gun at a volumetric ratio of 1 : 1 at each rate of 5 liter/m2 and they were kept for 6 minutes to deposit a metal layer on the glass plate by a chemical plating process.
  • Solution A6 :
  • Figure imgb0011
  • Solution B6:
  • Figure imgb0012
  • 0 The resulting metal layer had a thickness of 500 A and comprised about 100% of Cu (Ni was not substantially included). The characteristics of the layer were measured. The results are. shown in Table 1.
  • REFERENCE 2:
  • On the glass plate treated by the process of Reference 1, Solution A7 and Solution B7 were respectively sprayed by each spray-gun at a volumetric ratio of about 1 : 1 at each rate of 5 liter/m2 and they were kept for 2 minutes to deposit a nickel-boron alloy layer on the glass plate by a chemical plating.
  • Solution A7:
  • Figure imgb0013
  • Solution B7:
  • Figure imgb0014
  • The resulting nickel-boron alloy layer had a thickness of 0 500 A .
  • The characteristics of the nickel-boron layer were measured. The results are shown in Table 1.
  • REFERENCE 3:
    • On the glass plate treated by the process of Reference 1, Solution A8 and Solution B8 were respectively sprayed by each spray-gun at a volumetric ratio of about 1 : 1 at each rate of 5 liter/m2 and they were kept for 2 minutes to deposit a copper-boron alloy layer on the glass plate by a chemical plating.
    Solution A8:
  • Figure imgb0015
  • Solution B8:
  • Figure imgb0016
  • The resulting copper-boron alloy layer had a thickness of 500 Å.
  • The characteristics of the copper-boron layer were measured. The results are shown in Table 1.
    Figure imgb0017
  • As it is clearly found in Table 1, the heat radiation reflecting glass of the present invention had superior thermal characteristics such as heat passing coefficient and shading coefficient to those of the conventional heat-transfer reflecting glass having a nickel-boron alloy layer and also had superior durability to those of the copper layer and had neutral hue to be desirable as a heat, radiation reflecting glass.
  • The durability was determined by an observation of degree of corrosion after maintaining at 30°C RH of 70% for one month, ○ : non-corrosion X : corrosion
  • The visible transmissivity (Tv) was measured under the light incidence from each layer of the sample of glass plate having a thickness of 5 mm.
  • The visible reflectivity (Rv) was measured under the light incidence from the non-coated side of a glass plate coated with the layer having a thickness of 5 mm.
  • The heat-transfer coefficient (K value) and the shading coefficient (SC) were measured for an insulating glass unit prepared by a pair of glass plates having a thickness of 5 mm and an air space of 12 mm.
    • Figure 1 shows optical characteristics of the heat radiation reflecting glass of the present invention obtained in Example 2; and
    • Figure 2 shows optical characteristics of the heat radiation reflecting glass of the present invention obtained in Example 3.

Claims (9)

1) A heat radiation reflecting glass which comprises a transparent nickel-copper alloy layer formed by a chemical plating process on a glass plate.
2) The heat radiation reflecting glass according to Claim 1 wherein said transparent nickel-copper alloy layer comprises 1 to 25 wt.% of Ni component and 75 to 99 wt.% of Cu component.
3) The heat radiation reflecting glass according to Claim 1 wherein said transparent nickel-copper alloy layer comprises upto 100 ppm of Pd component.
4) The heat radiation reflecting glass according to Claim 1 wherein said transparent nickel-copper alloy layer comprises boron component.
5) The heat radiation reflecting glass according to Claim 4 wherein said transparent nickel-copper alloy layer comprises 1 to 20 wt.% of Ni component, 75 to 99 wt.% of Cu component, upto 5 wt.% of B component.
6) The heat radiation reflecting glass according to Claim 1 wherein said transparent nickel-copper alloy layer has a 0 thickness of 10 to 1000 A .
7) A process for preparing a heat radiation reflecting glass which comprises forming a nickel-copper alloy layer by applying a nickel salt, a copper salt and a reducing agent for reducing said salts in the presence of a palladium salt to chemically reduce said nickel salt and said copper salt.
8) The process according to Claim 7 wherein said reducing agent for reducing said nickel salt and copper salt is an alkali borohydride or a borane amine.
9) The process according to Claim 8 wherein said alkali borohydride is sodium borohydride.
EP81302669A 1981-06-15 1981-06-15 Heat radiation reflecting glass and preparation thereof Expired EP0067257B1 (en)

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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0307585A2 (en) * 1987-09-14 1989-03-22 Schering Aktiengesellschaft Process for the firmly adhering metallisation of an enamel
JP2009097085A (en) * 2007-09-25 2009-05-07 Hitachi Metals Ltd Cu ALLOY FILM FOR WIRING FILM, AND SPUTTERING TARGET MATERIAL FOR WIRING FILM FORMATION
WO2013057425A1 (en) 2011-10-21 2013-04-25 Saint-Gobain Glass France Solar control glazing comprising a layer of an alloy containing nicu
WO2017144828A1 (en) 2016-02-26 2017-08-31 Saint-Gobain Glass France Solar control glazing comprising a layer of a nicucr alloy

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FR1562312A (en) * 1967-03-11 1969-04-04
US3723155A (en) * 1970-07-23 1973-03-27 Ppg Industries Inc Wet chemical method of producing transparent metal films
DD109669A1 (en) * 1974-03-15 1974-11-12
US3962494A (en) * 1971-07-29 1976-06-08 Photocircuits Division Of Kollmorgan Corporation Sensitized substrates for chemical metallization
US4132832A (en) * 1976-10-12 1979-01-02 Nathan Feldstein Method of applying dispersions for activating non-conductors for electroless plating and article
US4158716A (en) * 1975-06-23 1979-06-19 Ppg Industries, Inc. Electrically nonconductive copper-boron coatings on nonmetallic substrates

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NL6804283A (en) * 1967-03-30 1968-10-01
EP0066656B1 (en) * 1981-06-02 1985-09-25 Asahi Glass Company Ltd. Process for preparing nickel layer

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Publication number Priority date Publication date Assignee Title
FR1562312A (en) * 1967-03-11 1969-04-04
US3723155A (en) * 1970-07-23 1973-03-27 Ppg Industries Inc Wet chemical method of producing transparent metal films
US3962494A (en) * 1971-07-29 1976-06-08 Photocircuits Division Of Kollmorgan Corporation Sensitized substrates for chemical metallization
DD109669A1 (en) * 1974-03-15 1974-11-12
US4158716A (en) * 1975-06-23 1979-06-19 Ppg Industries, Inc. Electrically nonconductive copper-boron coatings on nonmetallic substrates
US4132832A (en) * 1976-10-12 1979-01-02 Nathan Feldstein Method of applying dispersions for activating non-conductors for electroless plating and article

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0307585A2 (en) * 1987-09-14 1989-03-22 Schering Aktiengesellschaft Process for the firmly adhering metallisation of an enamel
EP0307585A3 (en) * 1987-09-14 1990-06-27 Schering Aktiengesellschaft Process for the firmly adhering metallisation of an enamel
JP2009097085A (en) * 2007-09-25 2009-05-07 Hitachi Metals Ltd Cu ALLOY FILM FOR WIRING FILM, AND SPUTTERING TARGET MATERIAL FOR WIRING FILM FORMATION
WO2013057425A1 (en) 2011-10-21 2013-04-25 Saint-Gobain Glass France Solar control glazing comprising a layer of an alloy containing nicu
US8889260B2 (en) 2011-10-21 2014-11-18 Saint-Gobain Glass France Solar control glazing comprising a layer of an alloy containing NiCu
WO2017144828A1 (en) 2016-02-26 2017-08-31 Saint-Gobain Glass France Solar control glazing comprising a layer of a nicucr alloy

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DE3173705D1 (en) 1986-03-20

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